• DocumentCode
    1566828
  • Title

    Culturing primary mouse embryonic fibroblasts in a microfluidic system

  • Author

    Villa, M.M. ; Pope, S.E. ; Conover, J.C. ; Fan, T.-H.

  • Author_Institution
    Dept. of Mech. Eng., Univ. of Connecticut, Storrs, CT
  • fYear
    2009
  • Firstpage
    1
  • Lastpage
    2
  • Abstract
    Primary mouse embryonic fibroblasts (mEFs) were cultured in a microfluidic system for a period of 8 days. The perfusion flow rate for these cells is different from those used for 3T3 fibroblasts and human adult fibroblasts due to the strong dependence on cell secreted factors. Primary mouse embryonic fibroblasts have not been cultured in a microfluidic system before. Our results have potential applications for these cells reprogrammed to a pluripotent state and important implications for primary cell culture using microdevices.
  • Keywords
    bioMEMS; biorheology; cellular biophysics; microfluidics; 3T3 fibroblasts; cell culturing; cell secretion factors; human adult fibroblasts; microdevices; microfluidic system; perfusion flow rate; pluripotent state; primary mouse embryonic fibroblasts; time 8 day; Cells (biology); Chemical analysis; Embryo; Fibroblasts; Glass; Medical control systems; Mice; Microfluidics; Plasma devices; Silicon;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioengineering Conference, 2009 IEEE 35th Annual Northeast
  • Conference_Location
    Boston, MA
  • Print_ISBN
    978-1-4244-4362-8
  • Electronic_ISBN
    978-1-4244-4364-2
  • Type

    conf

  • DOI
    10.1109/NEBC.2009.4967648
  • Filename
    4967648